Evidence map›Paper›PMID 33463257›Full record

ArticleACS biomaterials science & engineering2020

Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays.

Vittorio Ferrara, Giovanni Zito, Giuseppe Arrabito, Sebastiano Cataldo, Michelangelo Scopelliti, Carla Giordano, Valeria Vetri, Bruno Pignataro

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. On the Interaction between 1D Materials and Living Cells.Journal of functional biomaterials · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Vittorio FerraraDipartimento di Scienze Chimiche, Università di Catania, Viale A. Doria 6, 95125 Catania, Italy.
Giovanni ZitoDipartimento di Promozione della Salute, Materno-Infantile, Medicina Interna e Specialistica di Eccellenza "G. D'Alessandro" (ProMISE), Sezione di Malattie Endocrine, del Ricambio e della Nutrizione, Università di Palermo, Piazza delle Cliniche 2, 90127 Palermo, Sicilia, Italy.
Giuseppe ArrabitoDipartimento di Fisica e Chimica-Emilio Segrè, Università di Palermo, Viale delle Scienze, 90128 Palermo, Italy.ORCID 0000-0001-5890-5943
Sebastiano CataldoDipartimento di Fisica e Chimica-Emilio Segrè, Università di Palermo, Viale delle Scienze, 90128 Palermo, Italy.
Michelangelo ScopellitiDipartimento di Fisica e Chimica-Emilio Segrè, Università di Palermo, Viale delle Scienze, 90128 Palermo, Italy.ORCID 0000-0001-5931-7668
Carla GiordanoDipartimento di Promozione della Salute, Materno-Infantile, Medicina Interna e Specialistica di Eccellenza "G. D'Alessandro" (ProMISE), Sezione di Malattie Endocrine, del Ricambio e della Nutrizione, Università di Palermo, Piazza delle Cliniche 2, 90127 Palermo, Sicilia, Italy.
Valeria VetriDipartimento di Fisica e Chimica-Emilio Segrè, Università di Palermo, Viale delle Scienze, 90128 Palermo, Italy.ORCID 0000-0002-2307-1165
Bruno PignataroDipartimento di Fisica e Chimica-Emilio Segrè, Università di Palermo, Viale delle Scienze, 90128 Palermo, Italy.ORCID 0000-0003-3003-9144

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell microarrays are emerging tools to unravel intrinsic diversity within complex cell populations, opening up new approaches for the in-depth understanding of highly relevant diseases. However, most of the current methods for their fabrication are based on cumbersome patterning approaches, employing organic solvents and/or expensive materials. Here, we demonstrate an unprecedented green-chemistry strategy to produce single-cell capture biochips onto glass surfaces by all-aqueous inkjet printing. At first, a chitosan film is easily inkjet printed and immobilized onto hydroxyl-rich glass surfaces by electrostatic immobilization. In turn, poly(ethylene glycol) diglycidyl ether is grafted on the chitosan film to expose reactive epoxy groups and induce antifouling properties. Subsequently, microscale collagen spots are printed onto the above surface to define the attachment area for single adherent human cancer cells harvesting with high yield. The reported inkjet printing approach enables one to modulate the collagen area available for cell attachment in order to control the number of captured cells per spot, from single-cells up to double- and multiple-cell arrays. Proof-of-principle of the approach includes pharmacological treatment of single-cells by the model drug doxorubicin. The herein presented strategy for single-cell array fabrication can constitute a first step toward an innovative and environmentally friendly generation of aqueous-based inkjet-printed cellular devices.

Indexed as

GlassBiopolymersHumansMicroarray AnalysisBiopolymersbiointerfacebiopolymerinkjet printingmicroarraysingle-cell

Identifiers

PMID33463257
PMCPMC7997111

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.